| Year |
Citation |
Score |
| 2018 |
Pearl PL, Poduri A, Prabhu SP, Harini C, Goldstein R, Atkinson RM, Armstrong D, Kinney H. White matter spongiosis with vigabatrin therapy for infantile spasms. Epilepsia. PMID 29473152 DOI: 10.1111/Epi.14032 |
0.303 |
|
| 2010 |
Takei H, Wilfong A, Malphrus A, Yoshor D, Hunter JV, Armstrong DL, Bhattacharjee MB. Dual pathology in Rasmussen's encephalitis: a study of seven cases and review of the literature. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 30: 381-91. PMID 20051019 DOI: 10.1111/J.1440-1789.2009.01079.X |
0.315 |
|
| 2009 |
Blümcke I, Vinters HV, Armstrong D, Aronica E, Thom M, Spreafico R. Malformations of cortical development and epilepsies: neuropathological findings with emphasis on focal cortical dysplasia. Epileptic Disorders : International Epilepsy Journal With Videotape. 11: 181-93. PMID 19736171 DOI: 10.1684/Epd.2009.0261 |
0.322 |
|
| 2009 |
Chapleau CA, Calfa GD, Lane MC, Albertson AJ, Larimore JL, Kudo S, Armstrong DL, Percy AK, Pozzo-Miller L. Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations. Neurobiology of Disease. 35: 219-33. PMID 19442733 DOI: 10.1016/J.Nbd.2009.05.001 |
0.315 |
|
| 2008 |
Deguchi K, Clewing JM, Elizondo LI, Hirano R, Huang C, Choi K, Sloan EA, Lücke T, Marwedel KM, Powell RD, Santa Cruz K, Willaime-Morawek S, Inoue K, Lou S, Northrop JL, ... ... Armstrong DL, et al. Neurologic phenotype of Schimke immuno-osseous dysplasia and neurodevelopmental expression of SMARCAL1. Journal of Neuropathology and Experimental Neurology. 67: 565-77. PMID 18520775 DOI: 10.1097/Nen.0B013E3181772777 |
0.362 |
|
| 2007 |
Bi W, Yan J, Shi X, Yuva-Paylor LA, Antalffy BA, Goldman A, Yoo JW, Noebels JL, Armstrong DL, Paylor R, Lupski JR. Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes. Human Molecular Genetics. 16: 1802-13. PMID 17517686 DOI: 10.1093/Hmg/Ddm128 |
0.322 |
|
| 2007 |
Takei H, Wilfong A, Yoshor D, Armstrong DL, Bhattacharjee MB. Evidence of increased cell proliferation in the hippocampus in children with Ammon's horn sclerosis. Pathology International. 57: 76-81. PMID 17300671 DOI: 10.1111/J.1440-1827.2006.02060.X |
0.302 |
|
| 2007 |
Clewing JM, Antalfy BC, Lücke T, Najafian B, Marwedel KM, Hori A, Powel RM, Do AF, Najera L, SantaCruz K, Hicks MJ, Armstrong DL, Boerkoel CF. Schimke immuno-osseous dysplasia: a clinicopathological correlation. Journal of Medical Genetics. 44: 122-30. PMID 16840568 DOI: 10.1136/Jmg.2006.044313 |
0.303 |
|
| 2006 |
Patel MS, Becker LE, Toi A, Armstrong DL, Chitayat D. Severe, fetal-onset form of olivopontocerebellar hypoplasia in three sibs: PCH type 5? American Journal of Medical Genetics. Part A. 140: 594-603. PMID 16470708 DOI: 10.1002/Ajmg.A.31095 |
0.342 |
|
| 2005 |
Kilic SS, Donmez O, Sloan EA, Elizondo LI, Huang C, André JL, Bogdanovic R, Cockfield S, Cordeiro I, Deschenes G, Fründ S, Kaitila I, Lama G, Lamfers P, Lücke T, ... ... Armstrong D, et al. Association of migraine-like headaches with Schimke immuno-osseous dysplasia. American Journal of Medical Genetics. Part A. 135: 206-10. PMID 15884045 DOI: 10.1002/Ajmg.A.30692 |
0.317 |
|
| 2004 |
Collins AL, Levenson JM, Vilaythong AP, Richman R, Armstrong DL, Noebels JL, David Sweatt J, Zoghbi HY. Mild overexpression of MeCP2 causes a progressive neurological disorder in mice. Human Molecular Genetics. 13: 2679-89. PMID 15351775 DOI: 10.1093/Hmg/Ddh282 |
0.339 |
|
| 2004 |
Lorenzetti D, Antalffy B, Vogel H, Noveroske J, Armstrong D, Justice M. The neurological mutant quaking(viable) is Parkin deficient. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 15: 210-7. PMID 15014970 DOI: 10.1007/S00335-003-2333-5 |
0.311 |
|
| 2004 |
Moretti P, Blazo M, Garcia L, Armstrong D, Lewis RA, Roa B, Scaglia F. Spinocerebellar ataxia type 2 (SCA2) presenting with ophthalmoplegia and developmental delay in infancy. American Journal of Medical Genetics. Part A. 124: 392-6. PMID 14735588 DOI: 10.1002/Ajmg.A.20428 |
0.326 |
|
| 2003 |
Deguchi K, Inoue K, Avila WE, Lopez-Terrada D, Antalffy BA, Quattrocchi CC, Sheldon M, Mikoshiba K, D'Arcangelo G, Armstrong DL. Reelin and disabled-1 expression in developing and mature human cortical neurons. Journal of Neuropathology and Experimental Neurology. 62: 676-84. PMID 12834112 DOI: 10.1093/Jnen/62.6.676 |
0.312 |
|
| 2003 |
Yoo SY, Pennesi ME, Weeber EJ, Xu B, Atkinson R, Chen S, Armstrong DL, Wu SM, Sweatt JD, Zoghbi HY. SCA7 knockin mice model human SCA7 and reveal gradual accumulation of mutant ataxin-7 in neurons and abnormalities in short-term plasticity. Neuron. 37: 383-401. PMID 12575948 DOI: 10.1016/S0896-6273(02)01190-X |
0.329 |
|
| 2002 |
Shahbazian M, Young J, Yuva-Paylor L, Spencer C, Antalffy B, Noebels J, Armstrong D, Paylor R, Zoghbi H. Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3. Neuron. 35: 243-54. PMID 12160743 DOI: 10.1016/S0896-6273(02)00768-7 |
0.326 |
|
| 2002 |
Watase K, Weeber EJ, Xu B, Antalffy B, Yuva-Paylor L, Hashimoto K, Kano M, Atkinson R, Sun Y, Armstrong DL, Sweatt JD, Orr HT, Paylor R, Zoghbi HY. A long CAG repeat in the mouse Sca1 locus replicates SCA1 features and reveals the impact of protein solubility on selective neurodegeneration. Neuron. 34: 905-19. PMID 12086639 DOI: 10.1016/S0896-6273(02)00733-X |
0.338 |
|
| 2002 |
MarÃn-Padilla M, Parisi JE, Armstrong DL, Sargent SK, Kaplan JA. Shaken infant syndrome: developmental neuropathology, progressive cortical dysplasia, and epilepsy. Acta Neuropathologica. 103: 321-32. PMID 11904751 DOI: 10.1007/S00401-001-0470-Z |
0.314 |
|
| 2002 |
Shahbazian MD, Antalffy B, Armstrong DL, Zoghbi HY. Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation. Human Molecular Genetics. 11: 115-24. PMID 11809720 DOI: 10.1093/Hmg/11.2.115 |
0.333 |
|
| 2001 |
Deguchi K, Reyes C, Chakraborty S, Antalffy B, Glaze D, Armstrong D. Substance P immunoreactivity in the enteric nervous system in Rett syndrome Brain & Development. 23. PMID 11738858 DOI: 10.1016/S0387-7604(01)00360-6 |
0.302 |
|
| 2001 |
Parker JR, Armstrong DL, Strother D, Rudman DM, Dauser RC, Laurent JP, Deyd J, Rouah PE. Antineuronal nuclei immunohistochemical staining patterns in childhood ependymomas. Journal of Child Neurology. 16: 548-52. PMID 11510923 DOI: 10.1177/088307380101600802 |
0.309 |
|
| 2000 |
Yamamoto T, Armstrong D, Shibata N, Kato Y, Kobayashi M. Unique astrocytic inclusion in a 2 month-old baby showing Leigh-like brain lesions with lactic acidosis Brain and Development. 22: 234-238. PMID 10838110 DOI: 10.1016/S0387-7604(00)00117-0 |
0.308 |
|
| 1999 |
Tsai TF, Jiang YH, Bressler J, Armstrong D, Beaudet AL. Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome. Human Molecular Genetics. 8: 1357-64. PMID 10400982 DOI: 10.1093/Hmg/8.8.1357 |
0.306 |
|
| 1999 |
Yamamoto T, Armstrong D, Shibata N, Kanazawa M, Kobayashi M. Immature astrocytes in Fukuyama congenital muscular dystrophy: An immunohistochemical study Pediatric Neurology. 20: 31-37. PMID 10029257 DOI: 10.1016/S0887-8994(98)00089-7 |
0.309 |
|
| 1998 |
Jiang YH, Armstrong D, Albrecht U, Atkins CM, Noebels JL, Eichele G, Sweatt JD, Beaudet AL. Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation. Neuron. 21: 799-811. PMID 9808466 DOI: 10.1016/S0896-6273(00)80596-6 |
0.307 |
|
| 1998 |
Coerver KA, Gray SM, Barnes JE, Armstrong DL, McCabe ER. Developmental expression of hexokinase 1 and 3 in rats. Histochemistry and Cell Biology. 109: 75-86. PMID 9452958 DOI: 10.1007/S004180050204 |
0.307 |
|
| 1997 |
Clark GD, Mizuguchi M, Antalffy B, Barnes J, Armstrong D. Predominant localization of the LIS family of gene products to Cajal-Retzius cells and ventricular neuroepithelium in the developing human cortex. Journal of Neuropathology and Experimental Neurology. 56: 1044-52. PMID 9291945 DOI: 10.1097/00005072-199709000-00009 |
0.31 |
|
| 1997 |
Albrecht U, Sutcliffe JS, Cattanach BM, Beechey CV, Armstrong D, Eichele G, Beaudet AL. Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons. Nature Genetics. 17: 75-8. PMID 9288101 DOI: 10.1038/Ng0997-75 |
0.347 |
|
| 1994 |
Krishnan B, Armstrong DL, Grossman RG, Zhu ZQ, Rutecki PA, Mizrahi EM. Glial cell nuclear hypertrophy in complex partial seizures. Journal of Neuropathology and Experimental Neurology. 53: 502-7. PMID 8083691 DOI: 10.1097/00005072-199409000-00009 |
0.318 |
|
| 1993 |
Albrecht S, Schneider MC, Belmont J, Armstrong DL. Fatal infantile encephalopathy with olivopontocerebellar hypoplasia and micrencephaly. Report of three siblings. Acta Neuropathologica. 85: 394-9. PMID 8480512 DOI: 10.1007/Bf00334450 |
0.337 |
|
| 1990 |
Oldfors A, Sourander P, Armstrong DL, Percy AK, Witt-Engerström I, Hagberg BA. Rett syndrome: cerebellar pathology. Pediatric Neurology. 6: 310-4. PMID 2242172 DOI: 10.1016/0887-8994(90)90022-S |
0.328 |
|
| 1990 |
Zhu ZQ, Armstrong DL, Grossman RG, Hamilton WJ. Tyrosine hydroxylase-immunoreactive neurons in the temporal lobe in complex partial seizures. Annals of Neurology. 27: 564-72. PMID 1972875 DOI: 10.1002/Ana.410270518 |
0.304 |
|
| 1989 |
Dobyns WB, Pagon RA, Armstrong D, Curry CJ, Greenberg F, Grix A, Holmes LB, Laxova R, Michels VV, Robinow M. Diagnostic criteria for Walker-Warburg syndrome. American Journal of Medical Genetics. 32: 195-210. PMID 2494887 DOI: 10.1002/Ajmg.1320320213 |
0.337 |
|
| 1988 |
Jellinger K, Armstrong D, Zoghbi HY, Percy AK. Neuropathology of Rett syndrome. Acta Neuropathologica. 76: 142-58. PMID 2900587 DOI: 10.1007/Bf00688098 |
0.352 |
|
| 1984 |
Bagherian V, Graham M, Gerson LP, Armstrong DL. Double pituitary glands with partial duplication of facial and fore brain structures with hydrocephalus. Computerized Radiology : Official Journal of the Computerized Tomography Society. 8: 203-10. PMID 6478809 DOI: 10.1016/0730-4862(84)90124-0 |
0.314 |
|
| 1981 |
Takashima S, Becker LE, Armstrong DL, Chan F. Abnormal neuronal development in the visual cortex of the human fetus and infant with down's syndrome. A quantitative and qualitative Golgi study. Brain Research. 225: 1-21. PMID 6457667 DOI: 10.1016/0006-8993(81)90314-0 |
0.325 |
|
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